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Structural modeling of altered CLCN1 conformation following a novel mutation in a patient affected by autosomal dominant myotonia congenita (Thomsen disease).
Ferese R, Albano V, Falconi M, Iacovelli F, Campopiano R, Scala S, Griguoli AM, Gaglione A, Giardina E, Zampatti S, Storto M, Fornai F, D'Alessio C, Novelli G, Gambardella S. Ferese R, et al. Among authors: falconi m. Arch Ital Biol. 2017 Dec 1;155(4):118-130. doi: 10.12871/000398292017410. Arch Ital Biol. 2017. PMID: 29405036 No abstract available.
Molecular mechanism of statin-mediated LOX-1 inhibition.
Biocca S, Iacovelli F, Matarazzo S, Vindigni G, Oteri F, Desideri A, Falconi M. Biocca S, et al. Among authors: falconi m. Cell Cycle. 2015;14(10):1583-95. doi: 10.1080/15384101.2015.1026486. Cell Cycle. 2015. PMID: 25950192 Free PMC article.
1,089 results